# K190079: ArgenZ HT+

- Pathway: 510(k) (Traditional)
- Applicant: The Argen Corporation
- Decided: Apr 12, 2019 after 86 days
- Product code: EIH (Powder, Porcelain)
- Device class: 2
- Regulation: 21 CFR 872.6660
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K250393: ZircaGlow & ZircaGlow HT Zirconia (2025), 0 descendants of its own
- K201915: GenesisZr 4Y+ (ST1100) Zirconia (2021), 0 descendants of its own

Source page: https://510kreport.com/device/K190079
Methodology: https://510kreport.com/methodology